
Sign up to save your podcasts
Or
Teri McGrath, nurse and health educator, is very familiar with the paternalistic and misogynistic medical culture - in fact, her own physical symptoms were repeatedly dismissed by doctors until they discovered Teri was hyperthyroid. Turns out Teri’s symptoms weren’t ‘all in her pretty little head’, but actually stemming from an overactive thyroid that would have eventually killed her.
Today, Teri is taking on the behemoth medical system that routinely hides or denies medical harm and death, and the Goliath legal-medico system that effectively makes seeking compensation by medical error victims a traumatizing experience, financially draining, and an exercise in futility.
Canadian doctors have finagled themselves a pretty sweet deal: they have manipulated the political, legal and insurance systems so that when medical malpractice occurs, tax payers pay for the doctors high price lawyers. That is millions and millions of dollars each year coming out of tax payers pockets. The medical error victims - many of them too injured to work - are left to their own devices with no financial support for legal costs.
And what do these high price lawyers do? They fight the injured victims every step of the way, making it as hard - and expensive - and as long - as possible. The lawyers tactic is to bankrupt the injured victim before the case goes to court, or delay the court case in hopes the patient dies in the interim, thereby immediately ending the lawsuit.
No wonder fewer and fewer people trust their doctor. Or their politicians. They have set up the system so that medically injured patients are also emotionally traumatized and financially bankrupt. It is not by accident -- it is intentional and tactical to inflict more harm.
So Teri is on a mission to do 2 things: Make reporting of medical errors mandatory -- and increase access to compensation for medical error victims.
SHOW NOTES:
Be a podcast patron
Support Medical Error Interviews on Patreon by becoming a Patron for $2 / month for audio versions.
Premium Patrons get access to video versions of podcasts for $5 / month.
Be my Guest
I am always looking for guests to share their medical error experiences so we help bring awareness and make patients safer.
If you are a survivor, a victim’s surviving family member, a health care worker, advocate, researcher or policy maker and you would like to share your experiences, please send me an email with a brief description: [email protected]
Scott Simpson:
Counsellor + Patient Advocate + (former) Triathlete
I am a counsellor, patient advocate, and - before I became sick and disabled - a passionate triathlete. Work hard. Train hard. Rest hard.
I have been living with HIV since 1998. I was the first person living with HIV to compete at the triathlon world championships.
Thanks to research and access to medications, HIV is not a problem in my life.
I have been living with ME (myalgic encephalomyelitis) since 2012, and thanks in part to medical error, it is a big problem in my life.
Need a Counsellor?
Like me, many of my clients at Remedies Counseling have experienced the often devastating effects of medical error.
If you need a counsellor for your experience with medical error, or living with a chronic illness(es), I offer online video counseling appointments.
**For my health and life balance, I limit my number of counseling clients.**
Email me to learn more or book an appointment: [email protected]
Counseling / Research
I first became aware of the ubiquitousness of medical error during a decade of community based research working with the HIV Prevention Lab at Ryerson University, where I co-authored two research papers on a counseling intervention for people living with HIV, here and here.
Patient participants would often report varying degrees of medical neglect, error and harms as part of their counseling sessions.
Patient Advocacy
I am co-founder of the ME patient advocacy non-profit Millions Missing Canada, and on the Executive Committee of the Interdisciplinary Canadian Collaborative Myalgic Encephalomyelitis Research Network.
I am also a patient advisor for Health Quality Ontario’s Patient and Family Advisory Council, and member of Patients for Patient Safety Canada.
Medical Error Interviews podcast and vidcast emerged to give voice to victims, witnesses and participants in this hidden epidemic so we can create change toward a safer health care system.
My golden retriever Gladys is a constant source of love and joy. I hope to be well enough again one day to race triathlons again. Or even shovel the snow off the sidewalk.
3.6
1414 ratings
Teri McGrath, nurse and health educator, is very familiar with the paternalistic and misogynistic medical culture - in fact, her own physical symptoms were repeatedly dismissed by doctors until they discovered Teri was hyperthyroid. Turns out Teri’s symptoms weren’t ‘all in her pretty little head’, but actually stemming from an overactive thyroid that would have eventually killed her.
Today, Teri is taking on the behemoth medical system that routinely hides or denies medical harm and death, and the Goliath legal-medico system that effectively makes seeking compensation by medical error victims a traumatizing experience, financially draining, and an exercise in futility.
Canadian doctors have finagled themselves a pretty sweet deal: they have manipulated the political, legal and insurance systems so that when medical malpractice occurs, tax payers pay for the doctors high price lawyers. That is millions and millions of dollars each year coming out of tax payers pockets. The medical error victims - many of them too injured to work - are left to their own devices with no financial support for legal costs.
And what do these high price lawyers do? They fight the injured victims every step of the way, making it as hard - and expensive - and as long - as possible. The lawyers tactic is to bankrupt the injured victim before the case goes to court, or delay the court case in hopes the patient dies in the interim, thereby immediately ending the lawsuit.
No wonder fewer and fewer people trust their doctor. Or their politicians. They have set up the system so that medically injured patients are also emotionally traumatized and financially bankrupt. It is not by accident -- it is intentional and tactical to inflict more harm.
So Teri is on a mission to do 2 things: Make reporting of medical errors mandatory -- and increase access to compensation for medical error victims.
SHOW NOTES:
Be a podcast patron
Support Medical Error Interviews on Patreon by becoming a Patron for $2 / month for audio versions.
Premium Patrons get access to video versions of podcasts for $5 / month.
Be my Guest
I am always looking for guests to share their medical error experiences so we help bring awareness and make patients safer.
If you are a survivor, a victim’s surviving family member, a health care worker, advocate, researcher or policy maker and you would like to share your experiences, please send me an email with a brief description: [email protected]
Scott Simpson:
Counsellor + Patient Advocate + (former) Triathlete
I am a counsellor, patient advocate, and - before I became sick and disabled - a passionate triathlete. Work hard. Train hard. Rest hard.
I have been living with HIV since 1998. I was the first person living with HIV to compete at the triathlon world championships.
Thanks to research and access to medications, HIV is not a problem in my life.
I have been living with ME (myalgic encephalomyelitis) since 2012, and thanks in part to medical error, it is a big problem in my life.
Need a Counsellor?
Like me, many of my clients at Remedies Counseling have experienced the often devastating effects of medical error.
If you need a counsellor for your experience with medical error, or living with a chronic illness(es), I offer online video counseling appointments.
**For my health and life balance, I limit my number of counseling clients.**
Email me to learn more or book an appointment: [email protected]
Counseling / Research
I first became aware of the ubiquitousness of medical error during a decade of community based research working with the HIV Prevention Lab at Ryerson University, where I co-authored two research papers on a counseling intervention for people living with HIV, here and here.
Patient participants would often report varying degrees of medical neglect, error and harms as part of their counseling sessions.
Patient Advocacy
I am co-founder of the ME patient advocacy non-profit Millions Missing Canada, and on the Executive Committee of the Interdisciplinary Canadian Collaborative Myalgic Encephalomyelitis Research Network.
I am also a patient advisor for Health Quality Ontario’s Patient and Family Advisory Council, and member of Patients for Patient Safety Canada.
Medical Error Interviews podcast and vidcast emerged to give voice to victims, witnesses and participants in this hidden epidemic so we can create change toward a safer health care system.
My golden retriever Gladys is a constant source of love and joy. I hope to be well enough again one day to race triathlons again. Or even shovel the snow off the sidewalk.
484 Listeners